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BCAT-IN-2 is an inhibitor of mitochondrial branched-chain amino acid transaminase (BCAT2; IC50 = 50 nM in a cell-free assay).1 It increases serum levels of leucine, isoleucine, and valine in mice when administered at doses of 10, 30, or 100 mg/kg five hours prior to an amino acid bolus. BCAT-IN-2 also reduces tumor size and metastasis in a DU145 prostate cancer mouse xenograft model.2
WARNING This product is not for human or veterinary use.
1. The discovery of in vivo active mitochondrial branched-
2. BCAT2 binding to PCBP1 regulates the PI3K/AKT signaling pathway to inhibit autophagy-